Experience1-3 YearsRole OverviewThe Technical Documentation Engineer is responsible for the creation, validation, andmanagement of Production Support Documents (PSD) and Logistics Documents (LD), alongwith technical validation of compressor testing data, performance metrics, and sensorcalibration records. The role ensures accurate, compliant, and audit-ready technicaldocumentation.Key Responsibilities Create and maintain Production Support Documents
Job Description: Catalog Analyst Company: Randstad India(Payroll company)No od Position : 2Employment Type: 12 months renewable contractLocation: Bengaluru(WFH)Experience: 0-2 YearsShift: Day Shift (9:00 AM - 6:00 PM)Job Summary:We are looking for a highly motivated and detail-oriented Catalog Analyst to join our team in Chennai and Bangalore. The ideal candidate will play a critical role in maintaining the integrity and quality of our product catalog.
Prospective chart reviewers help to identify clinical alerts in a patients' history that may support an underlying diagnosis. These alerts are presented to a provider on a point-of-care tool to use during an encounter. This allows the condition to be addressed bythe clinician.Essential Job Functions:· Performs pre-visit medical record reviews to identify chronic conditions reported in prior years· Identify diagnoses that lack supporting documentation·
Job Description: Catalog Analyst Company: Randstad India(Payroll company)No od Position : 2Employment Type: 12 months renewable contractLocation: Chennai(Hybrid Work Model)Experience: 0-2 YearsShift: Day Shift (9:00 AM - 6:00 PM)Job Summary:We are looking for a highly motivated and detail-oriented Catalog Analyst to join our team in Chennai and Bangalore. The ideal candidate will play a critical role in maintaining the integrity and quality of our product
Job Title- Document Controller Job Location - Balewadi Pune Roles and Responsibilities Manage Governance level 1-2 projects independently as per applicable standards and procedures Supporting in maintaining Master Document List (MDL/MDR) consisting of all project related documents Examines project documents to verify completeness and accuracy of data as per project and contract requirements Maintaining a filing system in EDMS as per project
Job Title- Document Controller Job Location - Vilankurchi Road, Coimbatore - 641014, Tamilnadu, Roles and Responsibilities Manage Governance level 1-2 projects independently as per applicable standards and procedures Supporting in maintaining Master Document List (MDL/MDR) consisting of all project related documents Examines project documents to verify completeness and accuracy of data as per project and contract requirements Maintaining a filing
ob Description:Experience : 5-to-10-year Experience in Documentation ManagementEducation : Minimum Graduation in any StreamGood Communication & Collaboration SkillKey accountabilities:· Applies the rules defined in the Documentation Management Plan (DMP), Metadata· Controls documentation formal homogeneity: template, reference, version,· Controls contractual documentation according to customer requirements,· Assigns reference, when needed, to the
End-to-end ownership of abstract/congress/manuscript development To liaise with internal and external authors to develop and submit the various pub. vehicles Perform a literature search and prepare the summary of systematic literature searchPerform publication planning tasks: Support in developing scientific publications such as attending author group call, preparingminutes, target journal/congress selection, performing dummy submissions with
Key Responsibilities:Maintain accurate customer and account records in the system.Coordinate with Government authorities and internal teams for documentation requirements such as ECGC credit insurance, Duty Drawback, Marine Insurance, EDI Registration, Self-Sealing & Factory Stuffing documentation.Handle export-related compliance including IEC renewal, FIEO renewal, RCMC certification, and ECGC data submission for Star House status.Represent the company
Conduct comprehensive literature searches in PubMed, EMBASE, SCOPUS, and otherscientific databases.* Extract, organize, and maintain a structured scientific literature repository.* Develop study synopses and protocols in compliance with regulatory standards for bothclinical and preclinical research.* Perform technical review of Clinical Study Reports (CSRs) as per ICH guidelines.* Draft manuscripts in accordance with ICMJE, GPP4, and CONSORT
29 january 2026
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